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Encephalopfacial Angiomatosis



Encephalopfacial Angiomatosis Definition


Encephalopfacial angiomatosis, also referred to as Dimitiri disease or Struge-Weber syndrome, is a congenital defect that features clusters of blood vessel fibers and calcium deposits in the brain. Unusual facial birthmarks as well as seizures are common with persons in this condition. Angiomas also develop inside the face, brain, jaws and eyes.


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